Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274282Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-

https://huagongshe.com/de/reaction/274282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
EduktSodium hydrideHCID 24758—
Edukt3-Hydroxypropane-1-sulfonamideHCID 10486918—
Edukt6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-HCID 307380152,5%

Reaktionsschritte

In 12 ml of dimethylformamide was suspended 0.48 g of 60% sodium hydride in oil followed by addition of 0.835 g of 3-hydroxy-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperature for 30 minutes. Then, 0.928 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 18 hours. Following addition of 40 ml of ice water, the reaction mixture was adjusted to pH6 with 1N-hydrochloric acid then saturated with sodium chloride. The aqueous layer was extracted with tetrahydrofuran and the extract was dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from ethyl ether. The washed crystals were recrystallized from hot methanol to provide 0.811 g of title compound. m.p. 145°-147° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05389633
Quelldatensatzuspto-grants-1995_02
ORD IDord-ef5441d25a9b42f7b19df8c1f2556881
Quellennotizuspto-grants-1995_02